JP5371620B2 - Nuclear magnetic resonance imaging system - Google Patents

Description

  The present invention relates to a nuclear magnetic resonance imaging (MRI) apparatus that captures an image of a desired part of a subject using a nuclear magnetic resonance phenomenon, and more particularly to nuclear magnetic resonance imaging that prevents image quality deterioration due to heartbeat fluctuations. It relates to the device.

  The MRI device measures NMR signals generated by the spins of the subject, especially the tissues of the human body, and visualizes the form and function of the head, abdomen, limbs, etc. in two or three dimensions Device. In imaging, the NMR signal is given different phase encoding and frequency encoding depending on the gradient magnetic field. The measured NMR signal is reconstructed into an image by two-dimensional or three-dimensional Fourier transform.

Hereinafter, the outline of the prior art for the present invention will be described with reference to literature.
The heart moves by breathing and pulsation, and in order to compensate for the effects of these movements, the navigator echo method is used for breathing motion and the ECG gate method is used for pulsation. By taking images in synchronization as described above, artifacts due to body movement are prevented. However, even if the synchronization technique is applied, it is difficult to completely prevent artifacts due to respiration and heartbeat fluctuations.

  In order to prevent such image quality deterioration, a method as in Patent Document 1 has been proposed. In Patent Document 1, the repetition time of the excitation / collection procedure follows a small variation in the interval between the R wave and the R wave (hereinafter referred to as the RR interval), and the collected magnetic resonance signal is reconstructed when there is a large variation. Since it is excluded, magnetic resonance signals having substantially the same phase can be collected, and a high-quality electrocardiographic synchronization image free from artifacts can be obtained even when the RR interval fluctuates as in a heart disease patient. It becomes possible.

  A method as described in Non-Patent Document 1 has also been proposed. In Non-Patent Document 1, a good image without image quality degradation can be obtained by performing imaging while changing the data collection timing (Delay Time, hereinafter referred to as DT) in the expansion period in real time.

  However, in the above prior art, the data acquisition time (hereinafter referred to as AT) is not studied, and imaging is performed with a fixed value.

Japanese Patent No. 2880716

“Correction for Heart Rate Variability During 3D Whole Heart MR Coronary Angiography”, JMRI 27: 1046-1053 (2008)

In the method of Patent Document 1, since the collected magnetic resonance signal is excluded from the reconstruction process when there is a large fluctuation, the imaging time is extended. Considering the burden on the subject, it is not preferable to extend the imaging time. Further, in the method of Non-Patent Document 1, the data collection time AT is not examined. Therefore, as shown in FIG. 7, heart rate if you've vary significantly from the value parameter setting, it is possible that the data acquisition time AT _d diastole will span the next heartbeat and remain the same. As a result, the image quality is deteriorated and the imaging time is extended.

  An object of the present invention is to solve the problems of these known techniques, to prevent image quality deterioration when performing synchronous imaging, and to minimize the extension of imaging time.

The present invention provides parameterized data collection timing (DT _s ) during systole, data collection time (AT _s ) during systole, data collection timing (DT _d ) during diastole, data collection time during diastole Imaging is performed while changing (AT _d ) in real time.

Specifically, the nuclear magnetic resonance imaging apparatus of the present invention includes an electrocardiogram information detection means for detecting an electrocardiogram waveform of a subject, and DT _s , AT _s , DT _d , and, of the aT _d, and DT, aT calculation means for calculating a value including at least aT _d, the DT, with a value comprising at least aT _d calculated in aT calculation means, nuclear magnetic resonance signals from the subject And a measurement control means for controlling to measure.

Further, the nuclear magnetic resonance imaging apparatus of the present invention includes a parameter setting means for setting parameters of DT _s , AT _s , DT _d , and AT _d together with the heart rate of the subject, and an electrocardiographic waveform of the subject. Electrocardiogram information detection means for detecting, monitoring means for monitoring the heart rate of the subject based on the detected electrocardiogram waveform, a systolic period QT in the RR interval from the detected electrocardiogram waveform, and diastole QT, TQ calculating means for calculating the period TQ of the period, and DT _s , AT _s , DT _d , set by the parameter setting means based on the calculated systolic period QT, diastole period TQ, of the aT _d, set at least DT for calculating values that contain aT _d, aT calculation means and the heart rate of the subject was monitored by said monitoring means said parameter setting means If you are varied from the heart rate, _DT s set by said parameter setting _means, AT _s, DT _d, instead of the value of AT _d, comprising the DT, at least AT _d calculated in AT calculation means Measurement control means for controlling to measure a nuclear magnetic resonance signal from the subject using the value.

  In the present invention, the electrocardiogram information detecting means for detecting the electrocardiographic waveform of the subject may be an electrocardiograph or a pulse wave meter.

In the present invention, the measurement control means for controlling the measurement of the nuclear magnetic resonance signal from the subject monitors the filling rate of the k space, thereby reducing the phase according to the shortening or extension of AT _s and AT _d. Data may be collected by controlling encoding and slice encoding.

  According to the present invention, by performing imaging while changing both DT and AT corresponding to the electrocardiographic waveform of the subject, image quality deterioration when performing synchronous imaging is prevented, and imaging time is minimized. Can do.

The block diagram which shows the structure of the principal part of this invention The figure which shows the whole structure of the MRI apparatus with which this invention is applied The figure which shows the processing flow of this invention The figure which shows the relationship between RR interval and systole QT, diastole TQ Diagram showing AT shortening method for single echo system Diagram showing AT shortening method for multi-echo system Diagram showing problems with the prior art The figure which shows the effect which can be anticipated by this invention

  Hereinafter, preferred embodiments of the MRI apparatus of the present invention will be described in detail with reference to the accompanying drawings. Note that components having the same function are denoted by the same reference symbols throughout the drawings for describing the embodiments of the invention, and the repetitive description thereof is omitted.

  First, an overall outline of an example of the MRI apparatus according to the present invention will be described with reference to FIG. FIG. 2 is a block diagram showing the overall configuration of an embodiment of the MRI apparatus according to the present invention. This MRI apparatus obtains a tomographic image of a subject using the NMR phenomenon. As shown in FIG. 2, the MRI apparatus includes a static magnetic field generation system 2, a gradient magnetic field generation system 3, a transmission system 5, A reception system 6, a signal processing system 7, a sequencer 4, and a central processing unit (CPU) 8 are provided.

  The static magnetic field generation system 2 generates a uniform static magnetic field in the direction perpendicular to the body axis in the space around the subject 1 if the vertical magnetic field method is used, and in the direction of the body axis if the horizontal magnetic field method is used. Thus, a permanent magnet type, normal conducting type or superconducting type static magnetic field generating source is arranged around the subject 1.

  The gradient magnetic field generation system 3 includes a gradient magnetic field coil 9 wound in the three-axis directions of X, Y, and Z, which is a coordinate system (stationary coordinate system) of the MRI apparatus, and a gradient magnetic field power source 10 that drives each gradient magnetic field coil. The gradient magnetic fields Gx, Gy, Gz are applied in the three axial directions of X, Y, and Z by driving the gradient magnetic field power supply 10 of each coil in accordance with a command from the sequencer 4 described later. At the time of imaging, a slice direction gradient magnetic field pulse (Gs) is applied in a direction orthogonal to the slice plane (imaging cross section) to set a slice plane for the subject 1, and the remaining two orthogonal to the slice plane and orthogonal to each other A phase encoding direction gradient magnetic field pulse (Gp) and a frequency encoding direction gradient magnetic field pulse (Gf) are applied in one direction, and position information in each direction is encoded into an echo signal.

  The sequencer 4 is a control means that repeatedly applies a high-frequency magnetic field pulse (hereinafter referred to as “RF pulse”) and a gradient magnetic field pulse in a predetermined pulse sequence, and operates under the control of the CPU 8 to collect tomographic image data of the subject 1. Various commands necessary for the transmission are sent to the transmission system 5, the gradient magnetic field generation system 3, and the reception system 6.

  The transmission system 5 irradiates the subject 1 with RF pulses in order to cause nuclear magnetic resonance to occur in the nuclear spins of the atoms constituting the living tissue of the subject 1, and includes a high-frequency oscillator 11, a modulator 12, and a high-frequency amplifier. 13 and a high frequency coil (transmission coil) 14a on the transmission side. The high-frequency pulse output from the high-frequency oscillator 11 is amplitude-modulated by the modulator 12 at a timing according to a command from the sequencer 4, and the amplitude-modulated high-frequency pulse is amplified by the high-frequency amplifier 13 and then placed close to the subject 1. By supplying to the high frequency coil 14a, the subject 1 is irradiated with the RF pulse.

  The receiving system 6 detects an echo signal (NMR signal) emitted by nuclear magnetic resonance of nuclear spins constituting the biological tissue of the subject 1, and receives a high-frequency coil (receiving coil) 14b and a signal amplifier 15 on the receiving side. And a quadrature phase detector 16 and an A / D converter 17. After the NMR signal of the response of the subject 1 induced by the electromagnetic wave irradiated from the high frequency coil 14a on the transmission side is detected by the high frequency coil 14b arranged close to the subject 1 and amplified by the signal amplifier 15, The quadrature phase detector 16 divides the signal into two orthogonal signals at the timing according to the command from the sequencer 4, and each signal is converted into a digital quantity by the A / D converter 17 and sent to the signal processing system 7.

  The signal processing system 7 performs various data processing and display and storage of processing results. The signal processing system 7 includes an external storage device such as an optical disk 19 and a magnetic disk 18 and a display 20 including a CRT. Is input to the CPU 8, the CPU 8 executes processing such as signal processing and image reconstruction, and displays the tomographic image of the subject 1 as a result on the display 20, and the magnetic disk 18 of the external storage device. Record in etc.

  The operation unit 25 inputs various control information of the MRI apparatus and control information of processing performed in the signal processing system 7, and includes a trackball or mouse 23 and a keyboard 24. The operation unit 25 is disposed close to the display 20, and the operator controls various processes of the MRI apparatus interactively through the operation unit 25 while looking at the display 20.

  The high-frequency coil 14a and the gradient magnetic field coil 9 on the transmission side are placed in a static magnetic field space of the static magnetic field generation system 2 in which the subject 1 is inserted, and face the subject 1 in the case of the vertical magnetic field method. In the case of the method, it is installed so as to surround the subject 1. The high-frequency coil 14b on the receiving side is installed so as to face or surround the subject 1. Currently, the radionuclide to be imaged by the MRI apparatus is a hydrogen nucleus (proton) which is a main constituent material of the subject as widely used in clinical practice. By imaging information on the spatial distribution of proton density and the spatial distribution of relaxation time in the excited state, the form or function of the human head, abdomen, limbs, etc. is imaged two-dimensionally or three-dimensionally.

  The electrocardiogram electrode or pulse wave sensor 26, together with the electrocardiogram and pulse wave monitor 27, detects the electrocardiogram waveform of the subject 1, and constitutes an electrocardiogram information detection means.

  Next, examples of the present invention will be described. An example is a processing procedure for changing DT, AT, and period (Duration, hereinafter, the period of systole is QT and the period of diastole is TQ) during systole and diastole.

  First, FIG. 3 shows a flowchart in the present invention. In the present invention, Reference Scan is first performed (301). Reference Scan is performed to determine the heart rate, systole, and diastolic DT when performing synchronous imaging. The imaging sequence may be the same as the main imaging sequence, or may be the phase contrast method. Next, parameters (heart rate, DT) are set based on the information of Reference Scan (302), and when the parameters are set, QT, TQ using the formulas of Non-Patent Document 1 for the heart rate set by the parameters. Is calculated and stored (303). The relationship between the RR interval described in Non-Patent Document 1 and QT and TQ is shown in FIG. 4 and the calculation formula is shown below.

Here, T _rr'ave is an average of heartbeats (however, in the present invention, it is not a simple average but is weighted by the latest one heart rate)
κ ₁ = 0.375-0.390 (depends on healthy person, age and sex)
κ ₁ = 0.410 or 0.405 (heart patient, female, male)
κ ₂ = 0.07

Here, Tm ₀ is DT determined by Cine with high time resolution,
QT ₀ and TQ ₀ are constants with values obtained from T _rr (RR interval) during high-resolution Cine imaging when obtaining TM ₀ .

  Next, synchronous imaging (main imaging) is started (304). After the start of main imaging, the heart rate is monitored (305), and imaging is performed while comparing with the heart rate set with parameters (306). However, the heart rate used in the calculation formula of Non-Patent Document 1 is the average of the heart rates of the latest 5 heart beats, but in the present invention, it is not limited to the latest 5 heart beats (can be set by the user) Assume that the average heart rate is calculated by weighting the measured time. If the heart rate fluctuates as a result of the comparison, DT and AT at the next heart rate are changed (308), and data is collected (310). If there is no fluctuation in the heart rate, data collection is performed without changing the parameter-set DT and AT values (309). Steps (306) to (311) are repeated until the necessary amount of data is acquired. A method of determining completion of (311) will be described later. In the present invention, imaging is performed while changing DT and AT according to changes in heart rate, so that image quality deterioration can be prevented and imaging time can be minimized.

Next, FIG. 1 shows a block diagram of the main configuration of the nuclear magnetic resonance imaging apparatus of the present invention that implements this processing flow. The parameter setting means 101 determines the heart rate of the subject, the data collection timing DT _s during the systole, the data collection time AT _s during the systole, before starting the main imaging based on the reference scan information and the like. Values such as the data collection timing DT _{d in} the diastole and the data collection time AT _d in the diastole are set. The monitoring unit 102 monitors the heart rate of the subject based on the electrocardiographic waveform detected by the electrocardiogram information detection unit. The heart rate comparison means 103 compares the heart rate measured by the monitoring means 102 with the heart rate set by the parameter setting means 101, and outputs to the measurement control means 106 when the heart rate varies. . The QT and TQ calculating means 104 calculates the systolic period QT and the diastole period TQ in the RR interval from the electrocardiographic waveform detected by the electrocardiogram information detecting means. The DT, AT calculating means 105 calculates values such as DT _s , AT _s , DT _d , AT _d based on the systolic period QT and diastole period TQ calculated by the QT, TQ calculating means 104. Is to be calculated. The measurement control means 106 uses the values such as DT _s , AT _s , DT _d , AT _d set by the parameter setting means 101 and monitors by the monitoring means 102 based on the output of the heart rate comparison means 103. DT _s calculated by the DT, AT calculating means instead of the value set by the parameter setting means when the heart rate of the subject fluctuates from the heart rate set by the parameter setting means 101 The MRI apparatus is controlled to measure a nuclear magnetic resonance signal from the subject using values such as AT _s , DT _d , and AT _d .
Note that these configurations are configured as a part of the sequencer 4 and the CPU 8 in FIG. 2 and operate by a program, for example.

Next, a first embodiment will be described. The method of synchronization is ECG synchronization.
In the first embodiment, QT, TQ, and DT are calculated using the formula of Non-Patent Document 1 for the fluctuating heart rate. Since DT obtained in Non-Patent Document 1 is a value in the heart, it is necessary to consider a delay from the value of the heart when performing synchronous imaging of other parts such as the lower limbs.

According to Non-Patent Document 1, since QT generally does not change much even if the heart rate fluctuates, in Example 1, DT _s and AT _s are not changed from the time of parameter setting. AT _d is calculated by a ratio of TQ (hereinafter referred to as TQ _r ) obtained from the heart rate set as a parameter and TQ (hereinafter referred to as TQ _h ) obtained from the heart rate varied during the main imaging.
A specific calculation formula is the following formula (6).
AT _d = AT _{d, r} × TQ _r / TQ _h (6)
Where AT _{d, r} is the parameter data collection time
5 and 6 show how to shorten and extend AT. The AT shortening method differs between the single echo system and the multi-echo system. An example in the case of a single echo system is shown in FIG. Fig. 5 shows an example of the SSFP sequence. When the number of segments set by the parameter is 5, and the heart rate becomes faster, the AT is shortened by reducing the number of segments to 3 according to the change in the heart rate. It represents the situation. In this case, high-frequency data in k space is not acquired. When AT is extended, the number of Segments is increased and imaging is performed. Here, the Segment number is the number of data acquired within one heartbeat, and is the same as the segment scan segment that shoots by dividing the k-space into a plurality of segments.

  Next, an example in the case of a multi-echo system is shown in FIG. FIG. 6 shows an example in which the imaging sequence is fast spin echo (FSE). However, in the case of a multi-echo sequence, AT is shortened by not acquiring high-frequency data so that the effective TE does not change. . FIG. 6 shows the case where the number of echo trains set as a parameter is 7, and when the heart rate becomes fast, the AT is shortened by reducing the echo train number to 6 according to the change in the heart rate. Represents. When AT is extended, high frequency data that could not be acquired due to AT shortening may be acquired. 5 and 6 describe the case where the AT is shortened by thinning out only in the phase encoding direction, but depending on the imaging conditions, thinning out may be performed only in the slice encoding direction, or in both the phase encoding direction and the slice encoding direction. It may be thinned out.

  A determination method of data acquisition completion (311) and a data processing method will be described. Determination of completion of data acquisition is performed while monitoring the filling rate of the k space, and differs between a single-echo sequence and a multi-echo sequence. As an example, it is assumed that the parameters set in (302) are the phase encoding number 256 and 16 echoes / TR. In this case, 16TR is required to complete the data acquisition when the parameters are set. That is, it is necessary to repeat data collection 16 times. However, SSFP, which is a single echo sequence, may be able to complete the acquisition of the parameterized data amount with a smaller number of times than the scheduled number of repetitions when AT is frequently extended. Therefore, in the case of a single echo system sequence, the user can select whether to end when the acquisition of the data amount set by the parameter is completed or to repeat the acquisition of the initial number of repetitions even after the acquisition is completed. However, the number of repetitions does not exceed the number of parameters set. If data acquisition is repeated for the initial number of data acquisitions even after acquisition of the parameter-set data amount, zero encoded data is acquired for the remaining number of repetitions and added. If AT shortening occurs frequently, there may be high-frequency data that cannot be acquired. In such a case, estimation processing is performed.

  In FSE, which is a multi-echo sequence, it is necessary to acquire data so that the execution TE does not change. Therefore, data acquisition is repeated for a predetermined number of repetitions determined when the parameters are set. When AT shortening occurs, there is high-frequency data that cannot be acquired, but data may be acquired when AT is extended, or estimation processing may be performed.

  As described above, by changing the DT and AT of the systole and diastole during imaging, it is possible to always perform imaging with an appropriate cardiac phase and data collection time as shown in FIG. It is possible to prevent deterioration of image quality and extension of imaging time.

As a second embodiment, a case where the DT and AT during systole are also changed in the first embodiment will be described. QT is calculated for the fluctuating heart rate using the formula of Non-Patent Document 1. Next, a time that is half of the obtained QT is obtained and set as DT _s . A specific calculation formula is the following formula (7).
DT _s = QT _h / 2 (7)
However, QT _h is the Duration of systole obtained from the heart rate fluctuates.
In imaging of parts other than the heart, such as the lower limbs, it is necessary to consider the delay from the heart.
AT _s is calculated from the ratio of QT (hereinafter referred to as QT _r ) of the set heart rate and QT _{h in} the same manner as in diastole. A specific calculation formula is the following formula (8).
AT _s = AT _{s, r} × QT _r / QT _h (8)
However, AT _{s, r} is the data collection time set with parameters.

In the third embodiment, imaging is performed by reflecting the difference between the QT _r and TQ _r of the heart rate set with parameters and the QT _h and TQ _h of the heart rate changed during the main imaging as they are in the DT. The method of synchronization is ECG synchronization. AT is calculated from the ratio of QT and TQ, as in Examples 1 and 2. Also, the method for realizing the shortening and extension of AT is the same as that in the second embodiment. Specific calculation formulas are the following formulas (9) to (12).
_{DT s = DT s, r -} (QT r -QT h) ··· (9)
DT _d = DT _{d, r} − (TQ _r −TQ _h ) (10)
AT _s = AT _{s, r} × QT _r / QT _h (11)
AT _d = AT _{d, r} × TQ _r / TQ _h (12)
However, DT _{s, r} and DT _{d, r} are delay times with parameters set.

In the fourth embodiment, imaging is performed while changing DT and AT according to the ratio of the heart rate BR _r set as a parameter and the changed heart rate BR _h . The method of synchronization is ECG synchronization. Specific calculation formulas are the following formulas (13) to (16).
DT _s = DT _{s, r} × BR _r / BR _h (13)
DT _d = DT _{d, r} × BR _r / BR _h (14)
AT _s = AT _{s, r} × BR _r / BR _h (15)
AT _d = AT _{d, r} × BR _r / BR _h (16)

  In the fifth embodiment, the calculation method of QT and TQ for the changed heart rate is changed in the first to fourth embodiments. The method of synchronization is ECG synchronization. Specifically, a T wave is detected by the electrocardiogram information detection means. Here, if the CPU has the relationship between the T wave timing and the heart rate and TQ, QT in advance in the database, the TQ, QT can be obtained by detecting the T wave. When TQ and QT are obtained, DT and AT are calculated in the same manner as in Examples 1 to 4, and imaging is performed.

  In the sixth embodiment, the first to fourth embodiments are applied in pulse wave synchronous imaging. In pulse wave synchronous imaging, a pulse wave sensor 26 is attached to the fingertip, and measurement is performed by a pulse wave monitor 27. In Examples 1 to 4, the case of electrocardiographic synchronization imaging has been described. However, if the R-R interval is known, Non-Patent Document 1 can be used, so that it can also be applied to pulse wave synchronization imaging. However, in order to synchronize with the pulse wave (fingertip), it is necessary to consider the delay time from the heart.

1 ... subject, 2 ... static magnetic field generation system, 3 ... gradient magnetic field generation system, 4 ... sequencer, 5 ... transmission system, 6 ... reception system, 7 ... signal processing system, 8 ... central processing unit (CPU), 9 ... Gradient magnetic field coil, 10 ... Gradient magnetic field power supply, 11 ... High frequency transmitter, 12 ... Modulator, 13 ... High frequency amplifier, 14a ... High frequency coil (transmitting coil), 14b ... High frequency coil (receiving coil), 15 ... Signal amplifier, 16 ... Quadrature detector, 17 ... A / D converter, 18 ... Magnetic disk, 19 ... Optical disk, 20 ... Display, 21 ... ROM, 22 ... RAM, 23 ... Trackball or mouse, 24 ... Keyboard, 25 ... Operation unit 26 ... ECG electrode or pulse wave sensor, 27 ... ECG, pulse wave monitor,
101 ... parameter setting means, 102 ... monitoring means, 103 ... heart rate comparison means, 104 ... QT, TQ calculation means, 105 ... DT, AT calculation means, 106 ... measurement control means.

Claims (8)

Along with the heart rate of the subject, data collection timing during systole (hereinafter referred to as DT _s ), data collection time during systole (hereinafter referred to as AT _s ), data collection timing during diastole (hereinafter referred to as DT _d ), and Parameter setting means for parameter setting the value of data collection time (hereinafter referred to as AT _d ) during diastole;
Electrocardiogram information detection means for detecting an electrocardiogram waveform of the subject;
Monitoring means for monitoring the heart rate of the subject based on the detected electrocardiogram waveform;
QT, TQ calculating means for calculating a systole period QT and a diastole period TQ in the RR interval from the detected electrocardiogram waveform;
Based on the calculated systolic period QT and diastole period TQ, a value including at least AT _d is calculated from DT _s , AT _s , DT _d , and AT _d set by the parameter setting means. DT, AT calculation means to perform,
When the heart rate of the subject monitored by the monitoring unit varies from the heart rate set by the parameter setting unit, the values of DT _s , AT _s , DT _d , AT _d set by the parameter setting unit Instead of the measurement control means for controlling to measure a nuclear magnetic resonance signal from the subject using a value including at least AT _d calculated by the DT, AT calculation means,
A nuclear magnetic resonance imaging apparatus. The nuclear magnetic resonance imaging apparatus according to claim 1 .
The DT, AT calculating means calculates values of DT _s , AT _s , DT _d and AT _d ,
When the heart rate of the subject fluctuates from the heart rate set by the parameter setting unit, the measurement control unit includes items of DT _s , AT _s , DT _d and AT _d set by the parameter setting unit. Instead of the values, the DT _s , AT _s , DT _d and AT _d values calculated by the DT and AT calculating means are used to control to measure the nuclear magnetic resonance signal from the subject. A nuclear magnetic resonance imaging apparatus. The nuclear magnetic resonance imaging apparatus according to claim 1 .
The DT, AT calculation means includes a diastolic period (TQ _r ) and a diastolic data collection time (AT _{d, r} ) set by the parameter setting means, and a heart calculated by the QT, TQ calculation means. Based on the diastolic period (TQ _h ), the item value of AT _d is calculated,
When the heart rate of the subject fluctuates from the heart rate set by the parameter setting unit, the measurement control unit calculates the DT and AT instead of the AT _d value set by the parameter setting unit. A nuclear magnetic resonance imaging apparatus for measuring a nuclear magnetic resonance signal from a subject using the AT _d value calculated by the means. The nuclear magnetic resonance imaging apparatus according to claim 3 , further comprising:
The DT, AT calculation means includes a systolic period (QT _r ) and a systolic data collection time (AT _{s, r} ) set by the parameter setting means, and a heart calculated by the QT, TQ calculation means. Based on the period of systole (QT _h ), the values of DT _s and AT _s are calculated,
When the heart rate of the subject fluctuates from the heart rate set by the parameter setting unit, the measurement control unit replaces the values of DT _s and AT _s set by the parameter setting unit with the DT A nuclear magnetic resonance imaging apparatus for measuring a nuclear magnetic resonance signal from a subject using values of DT _s and AT _s calculated by an AT calculation means. The nuclear magnetic resonance imaging apparatus according to claim 1 .
The DT, AT calculation means includes a systolic data collection timing (DT _{s, r} ), a diastole data collection timing (DT _{d, r} ), and a systolic data collection time set by the parameter setting means. (AT _{s, r} ), diastole data collection time (AT _{d, r} ), systole period (QT _r ) and diastole period (TQ _r ), calculated by the QT, TQ calculation means The values of DT _s , AT _s , DT _d and AT _d are calculated based on the systolic period (QT _h ) and diastolic period (TQ _h ) ,
When the heart rate of the subject fluctuates from the heart rate set by the parameter setting unit, the measurement control unit determines the values of DT _s , AT _s , DT _d and AT _d set by the parameter setting unit. Instead, a nuclear magnetic resonance signal is measured from the subject using the values of DT _s , AT _s , DT _d and AT _d calculated by the DT and AT calculating means. Resonance imaging device. The nuclear magnetic resonance imaging apparatus according to claim 1 .
The DT, AT calculation means includes a systolic data collection timing (DT _{s, r} ), a diastole data collection timing (DT _{d, r} ), and a systolic data collection time set by the parameter setting means. Based on (AT _{s, r} ), diastole data collection time (AT _{d, r} ) and heart rate (BR _r ), and the measured heart rate (BR _h ) , DT _s , AT _s , DT _d And the value of AT _d ,
When the heart rate of the subject fluctuates from the heart rate set by the parameter setting unit, the measurement control unit determines the values of DT _s , AT _s , DT _d and AT _d set by the parameter setting unit. Instead, a nuclear magnetic resonance signal is measured from the subject using the values of DT _s , AT _s , DT _d and AT _d calculated by the DT and AT calculating means. Resonance imaging device. In nuclear magnetic resonance imaging apparatus according to claim 1 Symbol placement,
A nuclear magnetic resonance imaging apparatus, wherein the electrocardiogram information detection means for detecting an electrocardiogram waveform of the subject is an electrocardiograph or a pulse wave meter. In nuclear magnetic resonance imaging apparatus according to claim 1 Symbol placement,
The measurement control means for controlling to measure the nuclear magnetic resonance signal from the subject controls the phase encoding and slice encoding according to the shortening and extension of AT _s and AT _d by monitoring the filling rate of the k space. And collecting data, a nuclear magnetic resonance imaging apparatus.

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